Primary Device ID | 00840097503080 |
NIH Device Record Key | 87626641-02ac-4b22-a735-2d96147344c2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | restor3d Osteotomy Wedge |
Version Model Number | 1100-002-22140607 |
Company DUNS | 080819836 |
Company Name | Restor3d, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840097503080 [Primary] |
PLF | Bone Wedge |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2023-11-02 |
Device Publish Date | 2021-09-01 |
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00840097503080 | Titanium (Ti-6Al-4V) Cotton Wedge 002, Anatomic Footprint, 6mm Thickness |
00840097503073 | Titanium (Ti-6Al-4V) Cotton Wedge 002, Anatomic Footprint, 5mm Thickness |
00840097503028 | Titanium (Ti-6Al-4V) Cotton Wedge 002, Anatomic Footprint, 10mm Thickness |
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